Staphylococcus aureus endocarditis: a consequence of medical progress.

Published

Journal Article

CONTEXT: The global significance of infective endocarditis (IE) caused by Staphylococcus aureus is unknown. OBJECTIVES: To document the international emergence of health care-associated S aureus IE and methicillin-resistant S aureus (MRSA) IE and to evaluate regional variation in patients with S aureus IE. DESIGN, SETTING, AND PARTICIPANTS: Prospective observational cohort study set in 39 medical centers in 16 countries. Participants were a population of 1779 patients with definite IE as defined by Duke criteria who were enrolled in the International Collaboration on Endocarditis-Prospective Cohort Study from June 2000 to December 2003. MAIN OUTCOME MEASURE: In-hospital mortality. RESULTS: S aureus was the most common pathogen among the 1779 cases of definite IE in the International Collaboration on Endocarditis Prospective-Cohort Study (558 patients, 31.4%). Health care-associated infection was the most common form of S aureus IE (218 patients, 39.1%), accounting for 25.9% (Australia/New Zealand) to 54.2% (Brazil) of cases. Most patients with health care-associated S aureus IE (131 patients, 60.1%) acquired the infection outside of the hospital. MRSA IE was more common in the United States (37.2%) and Brazil (37.5%) than in Europe/Middle East (23.7%) and Australia/New Zealand (15.5%, P<.001). Persistent bacteremia was independently associated with MRSA IE (odds ratio, 6.2; 95% confidence interval, 2.9-13.2). Patients in the United States were most likely to be hemodialysis dependent, to have diabetes, to have a presumed intravascular device source, to receive vancomycin, to be infected with MRSA, and to have persistent bacteremia (P<.001 for all comparisons). CONCLUSIONS: S aureus is the leading cause of IE in many regions of the world. Characteristics of patients with S aureus IE vary significantly by region. Further studies are required to determine the causes of regional variation.

Full Text

Duke Authors

Cited Authors

  • Fowler, VG; Miro, JM; Hoen, B; Cabell, CH; Abrutyn, E; Rubinstein, E; Corey, GR; Spelman, D; Bradley, SF; Barsic, B; Pappas, PA; Anstrom, KJ; Wray, D; Fortes, CQ; Anguera, I; Athan, E; Jones, P; van der Meer, JTM; Elliott, TSJ; Levine, DP; Bayer, AS; ICE Investigators,

Published Date

  • June 22, 2005

Published In

Volume / Issue

  • 293 / 24

Start / End Page

  • 3012 - 3021

PubMed ID

  • 15972563

Pubmed Central ID

  • 15972563

Electronic International Standard Serial Number (EISSN)

  • 1538-3598

Digital Object Identifier (DOI)

  • 10.1001/jama.293.24.3012

Language

  • eng

Conference Location

  • United States